Piramal Pharma's Aurora unit completes USFDA inspection

Piramal Pharma announced that the US FDA conducted a general GMP (Good Manufacturing Practices) Inspection of Piramal Pharma's facility at Aurora, Canada from 26 May 2025 to 30 May 2025.

The inspection was completed successfully with Zero Form - 483 observations and No Action Indicated (NAI) designation.

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